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Validation of targeted sequencing of single-nucleotide polymorphisms for non-invasive prenatal detection of aneuploidy of chromosomes 13, 18, 21, X, and Y

Prenatal diagnosis, 2013-06, Vol.33 (6), p.575-579

2013

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Expanding non-invasive prenatal testing beyond chromosomes 21, 18, 13, X and Y

Clinical genetics, 2016-12, Vol.90 (6), p.477-485

Benn, P.

2016

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Aneuploidy screening by non‐invasive prenatal testing in twin pregnancy

Ultrasound in obstetrics & gynecology, 2017-04, Vol.49 (4), p.470-477

2017

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World Health Organization classification in combination with cytogenetic markers improves the prognostic stratification of patients with de novo primary myelodysplastic syndromes

British journal of haematology, 2007-05, Vol.137 (3), p.193-205

2007

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Gains, losses, and amplifications of genomic materials in primary gastric cancers analyzed by comparative genomic hybridization

Genes chromosomes & cancer, 1999-04, Vol.24 (4), p.299-305

1999

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Consistent chromosome abnormalities identify novel polymicrogyria loci in 1p36.3, 2p16.1-p23.1, 4q21.21-q22.1, 6q26-q27, and 21q2

American journal of medical genetics. Part A, 2008-07, Vol.146A (13), p.1637-1654

2008

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Genomic alterations associated with malignancy in head and neck cancer

Head & neck, 1998-03, Vol.20 (2), p.145-151

1998

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Linkage analysis confirms heterogeneity of hereditary gingival fibromatosis

Oral diseases, 2013-01, Vol.19 (1), p.100-105

2013

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Frequent amplification of 8q24, 11q, 17q, and 20q-specific genes in pancreatic cancer

Genes chromosomes & cancer, 2002-12, Vol.35 (4), p.353-358

2002

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Chromosome arm 20q gains and other genomic alterations in colorectal cancer metastatic to liver, as analyzed by comparative genomic hybridization and fluorescence in situ hybridization

Genes chromosomes & cancer, 1999-06, Vol.25 (2), p.82-90

1999

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Verification that common variation at 2q37.1, 6p25.3, 11q24.1, 15q23, and 19q13.32 influences chronic lymphocytic leukaemia risk

British journal of haematology, 2010-08, Vol.150 (4), p.473-479

2010

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Comparative genomic hybridization of squamous cell carcinoma of the esophagus: the possible involvement of the DPI gene in the 13q34 amplicon

Genes chromosomes & cancer, 1999-04, Vol.24 (4), p.337

1999

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Fusion of PDGFRB to MPRIP, CPSF6, and GOLGB1 in three patients with eosinophilia-associated myeloproliferative neoplasms

Genes chromosomes & cancer, 2015-12, Vol.54 (12), p.762-770

2015

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Genome-wide scan of bipolar disorder and investigation of population stratification effects on linkage: Support for susceptibility loci at 4q21, 7q36, 9p21, 12q24, 14q24, and 16p13

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2007-09, Vol.144B (6), p.791-801

2007

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Genetic abnormalities in mammary ductal intraepithelial neoplasia-flat type (clinging ductal carcinoma in situ) : A simulator of normal mammary epithelium

Cancer, 2000-05, Vol.88 (9), p.2072-2081

2000

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Toward localizing genes underlying cerebral asymmetry and mental health

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2005-05, Vol.135B (1), p.79-84

2005

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Spontaneous remission of infant acute myeloid leukemia with a novel four‐way translocation

Pediatric blood & cancer, 2020-02, Vol.67 (2), p.e28052-n/a

2020

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Association between histopathological features of dysplasia in oral leukoplakia and loss of heterozygosity

Histopathology, 2016-02, Vol.68 (3), p.456-460

2016

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Genetic Profiling by Single-Nucleotide Polymorphism-Based Array Analysis Defines Three Distinct Subtypes of Orbital Meningioma

Brain pathology (Zurich, Switzerland), 2015-03, Vol.25 (2), p.193-201

2015

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Aicardi‐Goutières syndrome: an important Mendelian mimic of congenital infection

Developmental medicine and child neurology, 2008-06, Vol.50 (6), p.410-416

2008

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Evidence for the multigenic inheritance of schizophrenia

American journal of medical genetics, 2001-12, Vol.105 (8), p.794-800

2001

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Allelotyping demonstrates common and distinct patterns of chromosomal loss in human lung cancer types

Genes chromosomes & cancer, 1998-04, Vol.21 (4), p.308-319

1998

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Molecular analysis of multifocal prostate cancer by comparative genomic hybridization

The Prostate, 2008-12, Vol.68 (16), p.1715-1724

2008

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Recurrence risks for trisomies 13, 18, and 21

American journal of medical genetics. Part A, 2009-12, Vol.149A (12), p.2716-2722

2009

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Validation of targeted sequencing of single-nucleotide polymorphisms for non-invasive prenatal detection of aneuploidy of chromosomes 13, 18, 21, X, and Y

Expanding non-invasive prenatal testing beyond chromosomes 21, 18, 13, X and Y

Aneuploidy screening by non‐invasive prenatal testing in twin pregnancy

World Health Organization classification in combination with cytogenetic markers improves the prognostic stratification of patients with de novo primary myelodysplastic syndromes

Gains, losses, and amplifications of genomic materials in primary gastric cancers analyzed by comparative genomic hybridization

Consistent chromosome abnormalities identify novel polymicrogyria loci in 1p36.3, 2p16.1-p23.1, 4q21.21-q22.1, 6q26-q27, and 21q2

Genomic alterations associated with malignancy in head and neck cancer

Linkage analysis confirms heterogeneity of hereditary gingival fibromatosis

The impact of cytogenetics on duration of response and overall survival in patients with relapsed multiple myeloma (long‐term follow‐up results from BSBMT/UKMF Myeloma X Relapse [Intensive]): a randomised, open‐label, phase 3 trial

Frequent amplification of 8q24, 11q, 17q, and 20q-specific genes in pancreatic cancer

Chromosome arm 20q gains and other genomic alterations in colorectal cancer metastatic to liver, as analyzed by comparative genomic hybridization and fluorescence in situ hybridization

Verification that common variation at 2q37.1, 6p25.3, 11q24.1, 15q23, and 19q13.32 influences chronic lymphocytic leukaemia risk

Comparative genomic hybridization of squamous cell carcinoma of the esophagus: the possible involvement of the DPI gene in the 13q34 amplicon

Fusion of PDGFRB to MPRIP, CPSF6, and GOLGB1 in three patients with eosinophilia-associated myeloproliferative neoplasms

Genome-wide scan of bipolar disorder and investigation of population stratification effects on linkage: Support for susceptibility loci at 4q21, 7q36, 9p21, 12q24, 14q24, and 16p13

Genetic abnormalities in mammary ductal intraepithelial neoplasia-flat type (clinging ductal carcinoma in situ) : A simulator of normal mammary epithelium

Toward localizing genes underlying cerebral asymmetry and mental health

Spontaneous remission of infant acute myeloid leukemia with a novel four‐way translocation

Association between histopathological features of dysplasia in oral leukoplakia and loss of heterozygosity

Genetic Profiling by Single-Nucleotide Polymorphism-Based Array Analysis Defines Three Distinct Subtypes of Orbital Meningioma

Aicardi‐Goutières syndrome: an important Mendelian mimic of congenital infection

Evidence for the multigenic inheritance of schizophrenia

Allelotyping demonstrates common and distinct patterns of chromosomal loss in human lung cancer types

Molecular analysis of multifocal prostate cancer by comparative genomic hybridization

Recurrence risks for trisomies 13, 18, and 21

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